Disease: Autism Spectrum Disorders
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16976358
LINC00907
0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 6
rs736707
LOC101927870 ; RELN
0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs7794745
CNTNAP2
0.851 0.040 7 146792514 intron variant A/T snv 0.49 6
rs1051312
SNAP25 ; SNAP25-AS1
0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 5
rs167771
DRD3
0.827 0.280 3 114157428 intron variant G/A;T snv 5
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 5
rs1060826
NOS2
0.851 0.160 17 27762841 synonymous variant T/C snv 0.66 0.67 4
rs1340513
KDM4C
0.882 0.120 9 6977633 intron variant G/A snv 0.75 4
rs1460808228
PRKCB
0.851 0.040 16 24185518 missense variant T/C snv 7.0E-06 4
rs1858830
MET
0.925 0.040 7 116672385 5 prime UTR variant C/G snv 0.40 4
rs2056202
SLC25A12
0.882 0.040 2 171855970 intron variant T/C snv 0.81 0.77 4
rs2736654
GLO1
0.882 0.120 6 38682852 missense variant T/A;G snv 4
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 3
rs201551401
GPR37
0.925 0.040 7 124746694 missense variant C/T snv 6.4E-05 1.4E-05 3
rs2292813
SLC25A12
0.882 0.040 2 171787719 intron variant T/C snv 0.81 3
rs362691
RELN
0.882 0.120 7 103610714 missense variant G/A;C;T snv 1.2E-05; 0.12 3
rs3747333
NLGN4X
0.925 0.040 X 5893491 missense variant G/A;C;T snv 7.6E-03 3
rs3747334
NLGN4X
0.925 0.040 X 5893489 synonymous variant G/A;C;T snv 1.2E-05; 6.7E-03 3
rs4141463
MACROD2
0.925 0.040 20 14766825 intron variant T/C snv 0.50 3
rs768913131
NRXN1
0.925 0.040 2 50552821 missense variant G/A snv 3
rs79667838
GRPR
0.882 0.120 X 16150432 missense variant C/T snv 3.0E-04 4.8E-04 3
rs10951154
HOTAIRM1 ; HOXA1
0.925 0.040 7 27095695 missense variant C/A;G;T snv 0.76 2
rs13000344 0.925 0.040 2 63062599 downstream gene variant T/G snv 0.11 2
rs1861972
EN2
0.925 0.040 7 155461298 intron variant G/A snv 0.72 2
rs1861973
EN2
0.925 0.040 7 155461450 intron variant T/C snv 0.73 2